Welcome to LookChem.com Sign In|Join Free
  • or
(tridecyloxy)acetic acid, with the chemical formula C13H26O3, is an organic compound categorized as a carboxylic acid. It features a long hydrocarbon chain comprising 13 carbon atoms and a terminal carboxyl group. This versatile chemical is valued for its ability to reduce the surface tension of liquids, facilitating easier mixing with water and other substances. Its unique properties also allow it to function as an effective emulsifier, surfactant, and dispersing agent.

6064-76-2

Post Buying Request

6064-76-2 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

6064-76-2 Usage

Uses

Used in Industrial and Personal Care Products:
(tridecyloxy)acetic acid is utilized as a surfactant and emulsifier in the industrial and personal care sectors. Its capacity to lower surface tension enables better mixing and blending of various ingredients, enhancing the performance and quality of the final products.
Used in Agricultural Formulations:
In the agricultural industry, (tridecyloxy)acetic acid serves as a valuable component in formulations. It aids in the even distribution of chemicals or particles within a solution, ensuring effective and consistent application to crops.
Used as a Dispersing Agent:
(tridecyloxy)acetic acid's ability to function as a dispersing agent makes it a sought-after ingredient in a wide range of applications. It helps in evenly distributing other chemicals or particles in a solution, leading to improved efficiency and performance in various industrial processes.

Check Digit Verification of cas no

The CAS Registry Mumber 6064-76-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,6 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6064-76:
(6*6)+(5*0)+(4*6)+(3*4)+(2*7)+(1*6)=92
92 % 10 = 2
So 6064-76-2 is a valid CAS Registry Number.

6064-76-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-tridecoxyacetic acid

1.2 Other means of identification

Product number -
Other names 3-Oxa-hexadecansaeure

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6064-76-2 SDS

6064-76-2Relevant academic research and scientific papers

Donepezil ether palmitate or its pharmaceutically acceptable salt

-

Paragraph 0102-0104; 0111-0113, (2021/03/23)

The present invention relates to novel donepezil ether palmitate or a pharmaceutically acceptable salt thereof, and a sustained-release pharmaceutical composition comprising the same as a main component. The donepezil ether palmitate of the present invention introduces an ether palmitate group to donepezil, thereby reducing the initial release of the active ingredient, donepezil, when administered in the body, reducing the risk of side effects such as drug toxicity, etc., and allowing uniform release of donepezil for long period of time to improve the drug treatment effect on dementia patients.

Long-chain triazolyl acids as inhibitors of osteoclastogenesis

Marshall, Andrew J.,Lin, Jian-Ming,Grey, Andrew,Reid, Ian R.,Cornish, Jillian,Denny, William A.

, p. 4112 - 4119 (2013/07/27)

Saturated fatty acids (e.g., palmitic acid) are known to moderately inhibit the development of osteoclasts in vitro. In pursuit of more effective inhibitors of osteoclastogenesis we explored two new classes of palmitic acid analogues containing either an ether or triazolyl group at various positions along the chain. The compounds were evaluated for their ability to inhibit the formation of osteoclasts in primary mouse bone marrow cultures. The oxyacids were generally prepared by condensation of the appropriate alkyl halides and diols, followed by Jones oxidation. The triazolyl acids were prepared by copper-catalysed click chemistry between alkyl azides and acetylenic acids, or with the appropriately-protected azides and alkynes, followed by deprotection and oxidation. The oxyacids were little more effective than palmitic acid, but the triazolyl analogues were much more effective osteoclastogenesis inhibitors, especially when the triazole was distant from the acid unit.

Contrast media for infarction and necrosis imaging

-

, (2008/06/13)

The invention relates to new compounds that are suitable as contrast media especially for infarction and necrosis imaging, process for their production and pharmaceutical agents that contain these compounds.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 6064-76-2